Ring-Opening Reactions of α- and β-Pinenes in Pressurized Hot Water in the Absence of Any Additive

Author:

Kawahara Tomomi1,Henmi Yui1,Onda Natsu1,Sato Toshiyuki1,Kawai-Nakamura Akiko1,Sue Kiwamu2,Iwamura Hiizu3,Hiaki Toshihiko1

Affiliation:

1. College of Industrial Technology, Nihon University, 1-2-1 Izumi-cho, Narashino, Chiba 275-8575, Japan

2. Nanosystem Research Institute, National Institute of Advanced Industrial Science and Technology, Tsukuba Central 5, 1-1-1 Higashi Tsukuba, Ibaraki 305-8565, Japan

3. College of Science and Technology, Nihon University, 1-8-14 Kanda-Surugadai, Chiyoda-ku, Tokyo 101-8308, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference42 articles.

1. Coppen, J. J. W.; Hone, G. A.Non–wood Forest Products 2, Gum Naval Stores: Turpentine and Rosin from Pine Resin; Natural Resources Inst., FAO of UN, FAO Corporate Document Repository, Rome, 1995. Another estimate is 263,000 tons in 1999 by: Morris, M.The Global Supply Position for Turpentine,Proceeding of Papers Presented at the IFEAT 2000 International Conference – Aroma Chemicals 2000 & Beyond;Florida, USA;29 Oct – 2 Nov 2000; pp17–31.

2. Zur Kenntniss der Terpene und der ätherischen Oele

3. Catalysis of gas and liquid phase ionic and radical rearrangements of α- and β-pinene by metal(IV) phosphate polymers

4. Kinetic and mechanistic aspects of myrcene production via thermal-induced β-pinene rearrangement

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